Evidence map›Paper›PMID 30323565›Full record

ArticleDrug design, development and therapy2018

Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway.

Lihong Chen, Jinhua Wang, Jianbo Wu, Qiaomei Zheng, Jifen Hu

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Indirubin alleviates CClIranian journal of basic medical sciences · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Role of lncRNA-ATB in ovarian cancer and its mechanisms of action.Experimental and therapeutic medicine · 2020
    Article
  14. Article
  15. Review
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Lihong ChenDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China, jifenhu_fj@126.com.
Jinhua WangDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China, jifenhu_fj@126.com.
Jianbo WuDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China, jifenhu_fj@126.com.
Qiaomei ZhengDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China, jifenhu_fj@126.com.
Jifen HuDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China, jifenhu_fj@126.com.
Fujian Medical University · CNFirst Affiliated Hospital of Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndirubin is the active component of Danggui Longhui Wan, a traditional Chinese medicine formulation. Due to its anti-inflammation and anti-tumor effects, indirubin has been widely used for the treatment of inflammation, cancer, and other chronic disease. Herein, we aimed to investigate the role and mechanism of indirubin in human ovarian cancer cell proliferation. MATERIALS AND

methodsThe cell viability was determined by Cell Counting Kit-8 and colony formation assays by treatment with different dosages of indirubin over 72 hours. Apoptosis was examined by flow cytometry with fluorescein isothiocyanate Annexin V Apoptosis Detection Kit. Western blot assay was finally applied to analyze the expression of cancer-related STAT3 pathway and its downstream proteins.

resultsIndirubin was found to significantly inhibit cell viability and induce apoptosis in 2 human ovarian cancer cell lines. Mechanistic studies revealed that indirubin treatment led to reduced levels of phosphorylated-STAT3, thus repressing the downstream pro-survival proteins and elevating pro-apoptosis ones.

conclusionOur study provided the evidence for anti-survival activity of indirubin by inhibiting cell viability and inducing apoptosis in human ovarian cancer cells, which involved impaired STAT3 signaling pathway. Our findings further support indirubin as a potential drug candidate against human ovarian cancer.

Indexed as

Antibiotics, AntineoplasticApoptosisCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorFemaleHumansIndolesOvarian NeoplasmsSignal TransductionSTAT3 Transcription FactorStructure-Activity RelationshipTumor Cells, CulturedAntibiotics, AntineoplasticindirubinIndolesSTAT3 protein, humanSTAT3 Transcription Factorcell viabilityindirubinovarian cancerSTAT3 signaling

Identifiers

PMID30323565
PMCPMC6174913
OpenAlexW2895415848

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.